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A rare complication of ventriculoperitoneal shunt: Pleural effusion without intrathoracic ventriculoperitoneal shunt catheter
BACKGROUND: Symptomatic pleural effusion following ventriculoperitoneal shunt (VPS) insertion is very rare and poorly understood in the literature in contrary to other mechanical complications. CASE DESCRIPTION: We report a case of 15 month-year-old girl who had VP shunt for congenital hydrocephalus...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Scientific Scholar
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7568093/ https://www.ncbi.nlm.nih.gov/pubmed/33093968 http://dx.doi.org/10.25259/SNI_57_2020 |
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author | Hilmani, Said Mesbahi, Tarek Bouaggad, Abderrahman Lakhdar, Abdelhakim |
author_facet | Hilmani, Said Mesbahi, Tarek Bouaggad, Abderrahman Lakhdar, Abdelhakim |
author_sort | Hilmani, Said |
collection | PubMed |
description | BACKGROUND: Symptomatic pleural effusion following ventriculoperitoneal shunt (VPS) insertion is very rare and poorly understood in the literature in contrary to other mechanical complications. CASE DESCRIPTION: We report a case of 15 month-year-old girl who had VP shunt for congenital hydrocephalus. Twelve months after surgery, she was diagnosed with massive hydrothorax. Chest X-ray and thoracoabdominal CT scan confirmed the right pleurisy and showed the tip of the peritoneal catheter in the general peritoneal cavity. We made thoracic drainage of the transudative pleural effusion. When we released the chest tube, 24 h after, the girl showed a respiratory distress again and the effusion resumed at the X-ray control. Her symptoms abated after the realization of a ventriculoatrial shunt “VAS.” Repeat chest X-ray confirmed the resolution of the hydrothorax. CONCLUSION: Despite the not yet well-understood mechanism of this rare and important VPS complication, management is simple based on X-ray confirmation, thoracentesis with biological analysis, and catheter replacement, especially in atrium “VAS.” |
format | Online Article Text |
id | pubmed-7568093 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Scientific Scholar |
record_format | MEDLINE/PubMed |
spelling | pubmed-75680932020-10-21 A rare complication of ventriculoperitoneal shunt: Pleural effusion without intrathoracic ventriculoperitoneal shunt catheter Hilmani, Said Mesbahi, Tarek Bouaggad, Abderrahman Lakhdar, Abdelhakim Surg Neurol Int Case Report BACKGROUND: Symptomatic pleural effusion following ventriculoperitoneal shunt (VPS) insertion is very rare and poorly understood in the literature in contrary to other mechanical complications. CASE DESCRIPTION: We report a case of 15 month-year-old girl who had VP shunt for congenital hydrocephalus. Twelve months after surgery, she was diagnosed with massive hydrothorax. Chest X-ray and thoracoabdominal CT scan confirmed the right pleurisy and showed the tip of the peritoneal catheter in the general peritoneal cavity. We made thoracic drainage of the transudative pleural effusion. When we released the chest tube, 24 h after, the girl showed a respiratory distress again and the effusion resumed at the X-ray control. Her symptoms abated after the realization of a ventriculoatrial shunt “VAS.” Repeat chest X-ray confirmed the resolution of the hydrothorax. CONCLUSION: Despite the not yet well-understood mechanism of this rare and important VPS complication, management is simple based on X-ray confirmation, thoracentesis with biological analysis, and catheter replacement, especially in atrium “VAS.” Scientific Scholar 2020-09-18 /pmc/articles/PMC7568093/ /pubmed/33093968 http://dx.doi.org/10.25259/SNI_57_2020 Text en Copyright: © 2020 Surgical Neurology International http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-Share Alike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Case Report Hilmani, Said Mesbahi, Tarek Bouaggad, Abderrahman Lakhdar, Abdelhakim A rare complication of ventriculoperitoneal shunt: Pleural effusion without intrathoracic ventriculoperitoneal shunt catheter |
title | A rare complication of ventriculoperitoneal shunt: Pleural effusion without intrathoracic ventriculoperitoneal shunt catheter |
title_full | A rare complication of ventriculoperitoneal shunt: Pleural effusion without intrathoracic ventriculoperitoneal shunt catheter |
title_fullStr | A rare complication of ventriculoperitoneal shunt: Pleural effusion without intrathoracic ventriculoperitoneal shunt catheter |
title_full_unstemmed | A rare complication of ventriculoperitoneal shunt: Pleural effusion without intrathoracic ventriculoperitoneal shunt catheter |
title_short | A rare complication of ventriculoperitoneal shunt: Pleural effusion without intrathoracic ventriculoperitoneal shunt catheter |
title_sort | rare complication of ventriculoperitoneal shunt: pleural effusion without intrathoracic ventriculoperitoneal shunt catheter |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7568093/ https://www.ncbi.nlm.nih.gov/pubmed/33093968 http://dx.doi.org/10.25259/SNI_57_2020 |
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